A Novel High-Pressure Monoclinic Metallic Phase of V2O3
arXiv:1312.7063 · doi:10.1103/PhysRevLett.112.056401
Abstract
Vanadium sesquioxide, V2O3, is a prototypical metal-to-insulator system where, in temperature-dependent studies, the transition always coincides with a corundum-to-monoclinic structural transition. As a function of pressure, V2O3 follows the expected behavior of increased metallicity due to a larger bandwidth for pressures up to 12.5 GPa. Surprisingly, for higher pressures when the structure becomes unstable, the resistance starts to increase. Around 32.5 GPa at 300 K, we observe a novel pressure-induced corundum-to-monoclinic transition between two metallic phases, showing that the structural phase transition can be decoupled from the metal-insulator transition. Using X-ray Raman scattering, we find that screening effects, which are strong in the corundum phase, become weakened at high pressures. Theoretical calculations indicate that this can be related to a decrease in coherent quasiparticle strength, suggesting that the high-pressure phase is likely a critical correlated metal, on the verge of Mott-insulating behavior.
The manuscript has been accepted by Physical Review Letters on Dec. 20 2013
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- Shining light on transition metal oxides: unveiling the hidden Fermi Liquid
- Pressure-Induced Confined Metal from the Mott Insulator Sr3Ir2O7
- Early-stage dynamics of metallic droplets embedded in the nanotextured Mott insulating phase of VO
- Low-temperature magnetic ordering and structural distortions in Vanadium Sesquioxide (VO)
- Disentangled cooperative orderings in artificial rare-earth nickelates
- How chromium doping affects the correlated electronic structure of V2O3
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